eudamed_udi
Primary ID: 04260681890543
AVERO Comfort (UDI 04260681890543)
Manufactured by BEKA-Hospitec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AVERO Comfort - Primary ID 04260681890543
Device Regulatory Overview
The AVERO Comfort (Model/Catalog Number: K122 BEKA Zubehöre für Pflegebadewannen) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification Y093399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K122 BEKA Zubehöre für Pflegebadewannen
- Product Code / EMDN
- Y093399
- Device Name
- AVERO Motion
- Database Sync Date
- 2026-08-09 16:46:38
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AVERO Comfort?
The registered manufacturer of record for AVERO Comfort is BEKA-Hospitec GmbH.
What is the Primary UDI-DI identifier for AVERO Comfort?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260681890543.
What classification code is assigned to this device?
This device is registered under product classification code Y093399.
Similar Classification Devices (Y093399)
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